Rapid Growth of Bi2Se3 Nanodots on MXene Nanosheets at Room Temperature for Promoting Sulfur Redox Kinetics.

Li-S batteries are hampered by problems with their cathodes and anodes simultaneously. The improvement of Li-S batteries needs to consider both the anode and cathode. Herein, a Bi2Se3@MXene composite is prepared for the first time by rapidly growing Bi2Se3 nanodots on two-dimensional (2D) MXene nanosheets at room temperature through simply adding high-reactive hydroxyethylthioselenide in Bi3+/MXene aqueous solution. Bi2Se3@MXene exhibits a 2D structure due to the template effect of 2D MXene. Bi2Se3@MXene can not only facilitate the conversion of lithium polysulfides (LiPSs) but also inhibit their shuttling in the S cathode due to its catalytic effect and adsorption force with LiPSs. Bi2Se3@MXene can also be used as an interfacial lithiophilic layer to inhibit Li dendrite growth in the Li metal anode. Theoretical calculations reveal that Bi2Se3 nanodots in Bi2Se3@MXene can effectively boost the adsorption ability with LiPSs, and the MXene in Bi2Se3@MXene can accelerate the electron transport. Under the bidirectional regulation of Bi2Se3@MXene in the Li metal anode and S cathode, the Li-S battery shows an enhanced electrochemical performance.

One-step growth of ultrathin CoSe2 nanobelts on N-doped MXene nanosheets for dendrite-inhibited and kinetic-accelerated lithium-sulfur chemistry.

The practical application of lithium-sulfur (Li-S) batteries is inhibited by the shuttle effect of lithium polysulfides (LiPSs) and slow polysulfide redox kinetics on the S cathode as well as the uncontrollable growth of dendrites on the Li metal anode. Therefore, both cathode and anode sides must be considered when modifying Li-S batteries. Herein, two-dimensional (2D) ultrathin CoSe2 nanobelts are in situ grown on 2D N-doped MXene nanosheets (CoSe2@N-MXene) via one-step solvothermal process for the first time. Owing to its unique 2D/2D structure, CoSe2@N-MXene can be processed to crumpled nanosheets by freeze-drying and flexible and freestanding films by vacuum filtration. These crumpled CoSe2@N-MXene nanosheets with abundant active sites and inner spaces can act as S hosts to accelerate polysulfide redox kinetics and suppress the shuttle effect of LiPSs owing to their strong adsorption ability and catalytic conversion effect with LiPSs. Meanwhile, the CoSe2@N-MXene film (CoSe2@NMF) can act as a current collector to promote uniform Li deposition because it contains lithiophilic CoSe2 and N sites. Under the systematic effect of CoSe2@N-MXene on S cathode and Li metal anode, the electrochemical and safety performance of Li-S batteries are improved. CoSe2@NMF also shows excellent storage performances in flexible energy storage devices.

Synchronous Regulation of D-Band Centers in Zn Substrates and Weakening Pauli Repulsion of Zn Ions Using the Ascorbic Acid Additive for Reversible Zinc Anodes.

The advanced aqueous zinc-ion batteries (AZIBs) are still challenging due to the harmful reactions including hydrogen evolution and corrosion. Here, a natural small molecule acid vitamin C (Vc) as an aqueous electrolyte additive has been selectively identified. The small molecule Vc can adjust the d band center of Zn substrate which fixes the active H+ so that the hydrogen evolution reaction (HER) is restrained. Simultaneously, it could also fine-tune the solvation structure of Zn ions due to the enhanced electrostatics and reduced Pauli repulsion verified by energy decomposition analysis (EDA). Hence, the cell retains an ultra-long cycle performance of over 1300 cycles and a superior Coulombic efficiency (CE) of 99.5 %. The prepared full cells display increased rate capability, cycle lifetime, and self-discharge suppression. Our results shed light on the mechanistic principle of electrolyte additives on the performance improvement of ZIBs, which is anticipated to render a new round of studies.

Heterogenization-Activated Zinc Telluride via Rectifying Interfacial Contact to Afford Synergistic Confinement-Adsorption-Catalysis for High-Performance Lithium-Sulfur Batteries.

The notorious shuttle effect and sluggish conversion kinetics of intermediate polysulfides (Li2S4, Li2S6, Li2S8) are severely hindered the large-scale development of Lithium-sulfur (Li-S) batteries. Rectifying interface effect has been a solution to regulate the electron distribution of catalysts via interfacial charge exchange. Herein, a ZnTe-ZnO heterojunction encapsulated in nitrogen-doped hierarchical porous carbon (ZnTe-O@NC) derived from metal-organic framework is fabricated. Theoretical calculations and experiments prove that the built-in electric field constructed at ZnTe-ZnO heterojunction via the rectifying interface contact, thus promoting the charge transfer as well as enhancing adsorption and conversion kinetics toward polysulfides, thereby stimulating the catalytic activity of the ZnTe. Meanwhile, the nitrogen-doped hierarchical porous carbon acts as confinement substrate also enables fast electrons/ions transport, combining with ZnTe-ZnO heterojunction realize a synergistic confinement-adsorption-catalysis toward polysulfides. As a result, the Li-S batteries with S/ZnTe-O@NC electrodes exhibit an impressive rate capability (639.7 mAh g-1 at 3 C) and cycling performance (70% capacity retention at 1 C over 500 cycles). Even with a high sulfur loading, it still delivers a superior electrochemical performance. This work provides a novel perspective on designing highly catalytic materials to achieve synergistic confinement-adsorption-catalysis for high-performance Li-S batteries.

MXene-Based Current Collectors for Advanced Rechargeable Batteries.

As an indispensable component of rechargeable batteries, the current collector plays a crucial role in supporting the electrode materials and collecting the accumulated electrical energy. However, some key issues, like uneven resources, high weight percentage, electrolytic corrosion, and high-voltage instability, cannot meet the growing need for rechargeable batteries. In recent years, MXene-based current collectors have achieved considerable achievements due to its unique structure, large surface area, and high conductivity. The related research has increased significantly. Nonetheless, a comprehensive review of this area is seldom. Herein the applications and progress of MXene in current collector are systematically summarized and discussed. Meanwhile, some challenges and future directions are presented.

In Situ Anchoring Ultrafine ZnS Nanodots on 2D MXene Nanosheets for Accelerating Polysulfide Redox and Regulating Li Plating.

Lithium-sulfur (Li-S) battery is a promising energy storage system due to its cost effectiveness and high energy density. However, formation of Li dendrites from Li metal anode and shuttle effect of lithium polysulfides (LiPSs) from S cathode impede its practical application. Herein, ultrafine ZnS nanodots are uniformly grown on 2D MXene nanosheets by a low-temperature (60 °C) hydrothermal method for the first time. Distinctively, the ZnS nanodot-decorated MXene nanosheets (ZnS/MXene) can be easily filtered to be a flexible and freestanding film in several minutes. The ZnS/MXene film can be used as a current collector for Li-metal anode to promote uniform Li deposition due to the superior lithiophilicity of ZnS nanodots. ZnS/MXene powders obtained by freeze drying can be used as separator decorator to address the shuttle effect of LiPSs due to their excellent adsorbability. Theoretical calculation proves that the existence of ZnS nanodots on MXene can obviously improve the adsorption ability of ZnS/MXene with Li+ and LiPSs. Li-S full cells with composite Li-metal anode and modified separator exhibit remarkable rate and cycling performance. Other transition metal sulfides (CdS, CuS, etc.) can be also grown on 2D MXene nanosheets by the low-temperature hydrothermal strategy.

Ultrastable and High-Rate 2D Siloxene Anode Enabled by Covalent Organic Framework Engineering for Advanced Lithium-Ion Batteries.

Siloxene as a new type of 2D material has wide potential applications due to its special structure. Especially, as anode for lithium-ion batteries, siloxene shows promising prospect due to its small volume change and low diffusion pathway. However, the unstable solid electrolyte interphase and low electronic conductivity lead to the low Coulombic efficiency, poor rate capability, and limited cycling performance. To settle the problems, a thin porous covalent organic framework (COF) coating layer is designed by in situ growth on micro-sized siloxene. With the inherent ionic conductive and electrolyte compatible advantages of COF, the engineered siloxene demonstrates superior electrochemical performance with 96% capacity retention at 8 A g-1 for 1500 cycles.

Sodiophilic Mg2+ -Decorated Ti3 C2 MXene for Dendrite-Free Sodium Metal Batteries with Carbonate-Based Electrolytes.

The advantages of sodium metal, such as abundant resources, low cost, high capacity, and high working potential, make it a promising metal anode. Unfortunately, the hazardous dendrite growth of sodium metal is one of the major hindrances for the practical application of sodium metal batteries (SMBs). By applying multifunctional Mg(II)@Ti3 C2 MXene as the protective layer for commercial Cu foil, the wettability of the electrolyte on the current collector is dramatically improved with the suppression of sodium dendrites. Moreover, the first-principles calculations prove that the surface of Mg(0001) is able to establish a connection with Na(111) growth, with Mg acting as the nucleation seed for sodium. The experimental results indicate that even when a high areal capacity of sodium (2 mAh cm-2 ) is deposited, no sodium dendrite is observed. Electrochemical tests, including symmetric cells, Na||Cu asymmetric cells, and full cells, prove the sodiophilic character of Mg2+ -decorated Ti3 C2 MXene. The results may also create a new pathway for developing other dendrite-free metal anodes, such as Li/K/Zn/Ca/Mg.

MXene/Organics Heterostructures Enable Ultrastable and High-Rate Lithium/Sodium Batteries.

Organic electrode materials have shown potential for rechargeable batteries because they are environmentally friendly, earth-abundant sources, recyclable, high sustainable, designable, flexible, and lightweight. However, low electrical conductivity and dissolution in organic liquid electrolytes hinder their further development. Herein, MXene/organics heterostructures are designed to address the problems of organic electrodes via a scalable and simple electrostatic self-assembly strategy. Under the effect of the electrostatic interaction, organic cathode material, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), is tightly attached to MXene nanosheets. Owing to the high electronic conductivity and special two-dimensional (2D) structure of MXene nanosheets, the issues of PTCDA cathode are effectively relieved. When applied in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs), the MXene@PTCDA heterostructure exhibits significantly enhanced rate capability and cycling performance than bare PTCDA. The heterostructures proposed here can be applied to other (K, Zn, Al, Mg, Ca, etc.) battery systems. In addition to energy storage and conversion, the heterostructures can be also extended to many fields such as catalysis, sensors, electronics, optics, membranes, semiconductors, biomedicines, etc.

Scalable Synthesis of Nano-Sized Bi for Separator Modifying in 5V-Class Lithium Metal Batteries and Potassium Ion Batteries Anodes.

With the advantages of high theoretical-specific capacity and lowest working potential, lithium metal anode is considered as the most promising anode for next-generation batteries. Here, a scalable dealloying method is developed to prepare nano-sized bismuth (Bi). It is found that the Bi-modification can not only enhance the wettability of the commercial polyethylene separator but also suppresses the lithium dendrite growth. With the nano-sized Bi modified separator, 5V-class lithium metal batteries with commercial carbonate-based electrolyte show a 91% capacity retention ratio after 800 cycles. First-principle calculations prove that lithium atoms tend to deposit smoothly on the Bi surface. Moreover, for potassium ion batteries, nano-sized Bi shows a stable cycling performance and high capacity. The results may be useful for the development of high-energy and high-safety batteries.

High-Safety and Dendrite-Free Lithium Metal Batteries Enabled by Building a Stable Interface in a Nonflammable Medium-Concentration Phosphate Electrolyte.

Lithium metal anodes are promising for their high energy density and low working potential. However, high reactivity and dendrite growth of lithium metal lead to serious safety issues. Lithium dendrite may form "dead lithium" or pierce the separator, which will cause low efficiency and short-circuit inside the battery. A nonflammable phosphate-based electrolyte can effectively solve the flammability problem. Also, it shows poor compatibility with lithium metal anodes, resulting in an unstable solid electrolyte interface (SEI), which leads to dendrite growth and poor electrochemical performance. In this study, trimethyl phosphate is used to ensure the safety of lithium metal batteries. By adjusting the concentration of lithium salt and introducing fluoroethylene carbonate, a stable SEI layer is formed on the surface of the lithium metal anode and dendrite growth of the lithium metal anode is inhibited. Lithium metal batteries with a modified electrolyte achieved stable electrochemical plating/stripping, and the full cell has 93.4% capacity left and the coulombic efficiency is nearly 100%. In addition, the modified electrolyte can also enable reversible intercalation and de-intercalation of Li+ in the commercial graphite anode. This work may provide an alternative direction for the development of lithium metal batteries with high safety and high energy density.

Covalent Organic Frameworks and Their Derivatives for Better Metal Anodes in Rechargeable Batteries.

Metal anodes based on a plating/stripping electrochemistry such as metallic Li, Na, K, Zn, Ca, Mg, Fe, and Al are recognized as promising anode materials for constructing next-generation high-energy-density rechargeable metal batteries owing to their low electrochemical potential, high theoretical specific capacity, superior electronic conductivity, etc. However, inherent issues such as high chemical reactivity, severe growth of dendrites, huge volume changes, and unstable interface largely impede their practical application. Covalent organic frameworks (COFs) and their derivatives as emerging multifunctional materials have already well addressed the inherent issues of metal anodes in the past several years due to their abundant metallophilic functional groups, special inner channels, and controllable structures. COFs and their derivatives can solve the issues of metal anodes by interfacial modification, homogenizing ion flux, acting as nucleation seeds, reducing the corrosion of metal anodes, and so on. Nevertheless, related reviews are still absent. Here we present a detailed review of multifunctional COFs and their derivatives in metal anodes for rechargeable metal batteries. Meanwhile, some outlooks and opinions are put forward. We believe the review can catch the eyes of relevant researchers and supply some inspiration for future research.

Design of Robust, Lithiophilic, and Flexible Inorganic-Polymer Protective Layer by Separator Engineering Enables Dendrite-Free Lithium Metal Batteries with LiNi0.8 Mn0.1 Co0.1 O2 Cathode.

As a promising candidate for the high energy density cells, the practical application of lithium-metal batteries (LMBs) is still extremely hindered by the uncontrolled growth of lithium (Li) dendrites. Herein, a facile strategy is developed that enables dendrite-free Li deposition by coating highly-lithiophilic amorphous SiO microparticles combined with high-binding polyacrylate acid (SiO@PAA) on polyethylene separators. A lithiated SiO and PAA (lithiated-SiO/PAA) protective layer with synergistic flexible and robust features is formed on the Li metal anode via the in situ reaction to offer outstanding interfacial stability during long-term cycles. By suppressing the formation of dead Li and random Li deposition, reducing the side reaction, and buffering the volume changes during the lithium deposition and dissolution, such a protective layer realizes a dendrite-free morphology of Li metal anode. Furthermore, sufficient ionic conductivity, uniform lithium-ion flux, and interface adaptability is guaranteed by the lithiated-SiO and Li polyacrylate acid. As a result, Li metal anodes display significantly enhanced cycling stability and coulombic efficiency in Li||Li and Cu||Li cells. When the composite separator is applied in a full cell with a carbonate-based electrolyte and LiNi0.8 Mn0.1 Co0.1 O2 cathode, it exhibits three times longer lifespan than control cell at current density of 5 C.

High-Safety and High-Voltage Lithium Metal Batteries Enabled by a Nonflammable Ether-Based Electrolyte with Phosphazene as a Cosolvent.

The high reactivity between lithium metal and traditional carbonate electrolytes is a great obstacle to realize the long-term cycling ability of lithium metal batteries. Ether-based electrolytes have good stability toward lithium metal anodes. However, the oxidation stability of ether-based electrolytes is generally lower than 4 V, which limits the application of high-voltage (>4 V) cathodes and restricts the energy density. The high flammability of ether is another key issue that hinders the commercialization of ether-based electrolytes. To address these issues, herein, we report a high-voltage, nonflammable ether-based electrolyte with F-, N-, and P-rich hexafluorocyclotriphosphazene (HFPN) as a cosolvent. HFPN can not only act as a highly efficient flame-retarding agent but also form a dense and homogeneous solid electrolyte interphase (SEI) layer rich in LiF and Li3N on the lithium metal anode, which stabilizes the lithium/electrolyte interface and inhibits the formation of lithium dendrites. Moreover, the HFPN-based electrolyte has a wider potential window than 4 V. As a result, with this electrolyte, high-voltage lithium metal batteries exhibit a capacity retention of ∼95% after 100 cycles. This study may provide a new pathway for developing safe, high-energy, and dendrite-free lithium metal batteries.

Two-Dimensional Silicon/Carbon from Commercial Alloy and CO2 for Lithium Storage and Flexible Ti3C2Tx MXene-Based Lithium-Metal Batteries.

Silicon has been considered as the most promising anode candidate for next-generation lithium-ion batteries. However, the fast capacity decay caused by huge volume expansion and low electronic conductivity limit the electrochemical performance. Herein, atomic distributed, air-stable, layer-by-layer-assembled Si/C (L-Si/C) is designed and in situ constructed from commercial micron-sized layered CaSi2 alloy with the greenhouse gas CO2. The inner structure of Si as well as the content and graphitization of C can be regulated by simply adjusting the reaction conditions. The rationally designed layered structure can enhance electronic conductivity and mitigate volume change without disrupting the carbon layer or destroying the solid electrolyte interface. Moreover, the single-layer Si and C can enhance lithium-ion transport in active materials. With these advantages, L-Si/C anode delivers an 82.85% capacity retention even after 3200 cycles and superior rate performance. The battery-capacitance dual-model mechanism is certified via quantitative kinetics measurement. Besides, the self-standing architecture is designed via assembling L-Si/C and MXene. Lithiophilic L-Si/C can guide homogeneous Li deposition with alleviated volume change. With the MXene/L-Si/C host for lithium-metal batteries, an ultralong life span up to 500 h in a carbonate-based electrolyte is achieved. A full cell with a high-energy 5 V LiNi0.5Mn1.5O4 cathode is constructed to verify the practicality of L-Si/C and MXene/L-Si/C. The rational design of a special layer structure may propose a strategy for other materials and energy storage systems.

Stable Lithium Anode of Li-O2 Batteries in a Wet Electrolyte Enabled by a High-Current Treatment.

Rechargeable Li-air (O2) batteries have attracted a great deal of attention because of their high theoretical energy density and been regarded as a promising next-generation energy storage technology. Among numerous obstacles to Li-air (O2) batteries preventing their use in practical applications, water is a representative impurity for Li-air (O2), which could hasten the deterioration of the anode and accelarate the premature death of cells. Here, we report an effective in situ high-current pretreatment process to enhance the cycling performance of Li-O2 batteries in a wet tetraethylene glycol dimethyl ether-based electrolyte. With the help of certain levels of H2O (from 100 to 2000 ppm) in the electrolyte, adequate Li2O formed on the lithium anode surface after high-current pretreatment, which is necessary for a robust and uniform solid electrolyte interphase layer to protect Li metal during the long-term discharge-charge cycling process. This in situ high-current pretreatment method in a wet electrolyte is shown to be an effective approach for enhancing the cycling performance of Li-O2 batteries with a stable Li metal anode and promoting the realization of practical Li-air batteries.

Scalable and Physical Synthesis of 2D Silicon from Bulk Layered Alloy for Lithium-Ion Batteries and Lithium Metal Batteries.

Owing to its distinctive structure and properties, 2D silicon (2DSi) has been widely applied in hydrogen storage, sensors, electronic device, catalysis, electrochemical energy storage, etc. However, scalable and low-cost fabrication of high-quality 2DSi remains a great challenge. In this work, a physical vacuum distillation method is designed to obtain high-quality 2DSi from a bulk layered calcium-silicon alloy. With this method, the lower boiling point calcium metal is evaporated to construct 2DSi and can be further recycled. The effect of vacuum conditions on morphology, components, and electrochemical properties is further explored. As an anode for lithium-ion batteries, the 2DSi delivers a stable cyclability of 835 mAh g-1 after 3000 cycles at 5000 mA g-1 (0.003025% capacity decay per cycle). The electrochemical performance enhancing mechanism is also probed. In addition, a 2D/2D flexible and binder-free paper by combining 2DSi with 2D MXene is constructed. As a lithiophilic nuclear agent for lithium metal anodes, the 2DSi can efficiently suppress the Li dendrite growth and reduce nucleation barriers, achieving a high Coulombic efficiency (98% at 1 mA cm-2, 97% at 2 mA cm-2) around 600 cycles and a long lifespan of 1000 h. The crystal growth difference of lithium metal on Cu foil and 2DSi is studied. This work may provide a pathway for green, low-cost, and scalable synthesis of 2D materials.

Room-Temperature Liquid Metal Confined in MXene Paper as a Flexible, Freestanding, and Binder-Free Anode for Next-Generation Lithium-Ion Batteries.

Exploring flexible lithium-ion batteries is required with the ever-increasing demand for wearable and portable electronic devices. Selecting a flexible conductive substrate accompanying with closely coupled active materials is the key point. Here, a lightweight, flexible, and freestanding MXene/liquid metal paper is fabricated by confining 3 °C GaInSnZn liquid metal in the matrix of MXene paper without any binder or conductive additive. When used as anode for lithium-ion cells, it can deliver a high discharge capacity of 638.79 mAh g-1 at 20 mA g-1 . It also exhibits satisfactory rate capacities, with discharge capacities of 507.42, 483.33, 480.22, 452.30, and 404.47 mAh g-1 at 50, 100, 200, 500, and 1000 mA g-1 , respectively. The cycling performance is obviously improved by slightly reducing the charge-discharge voltage range. The composite paper also has better electrochemical performance than liquid metal coated Cu foil. This study proposes a novel flexible anode by a clever combination of MXene paper and low-melting point liquid metal, paving the way for next-generation lithium-ion batteries.

Flexible and Free-Standing Ti3C2Tx MXene@Zn Paper for Dendrite-Free Aqueous Zinc Metal Batteries and Nonaqueous Lithium Metal Batteries.

Dendrite growth of metal anodes is one of the key hindrances for both secondary aqueous metal batteries and nonaqueous metal batteries. In this work, a freestanding Ti3C2Tx MXene@Zn paper is designed as both zinc metal anode and lithium metal anode host to address the issue. The binder-free Ti3C2Tx MXene@Zn paper exhibits merits of good mechanical flexibility, high electronic conductivity, hydrophilicity, and lithiophilicity. The crystal growth mechanism of Zn metal on common Zn foil and Ti3C2Tx MXene@Zn composite is also studied. It is found that the Ti3C2Tx MXene@Zn paper can effectively suppress the dendrite growth of Zn, enabling reversible and fast Zn plating/stripping kinetics in an aqueous electrolyte. Moreover, the Ti3C2Tx MXene@Zn paper can be used as a 3D host for a lithium metal anode. In this host, Zn is utilized as a nucleation agent to suppress the Li dendrite growth. The freestanding Ti3C2Tx MXene@Zn@Li anode exhibits superior reversibility with high Coulombic efficiency (97.69% over 600 cycles at 1.0 mA cm-2) and low polarization compared with the Cu@Li anode. These findings may be useful for the design of dendrite-free metal-based energy storage systems.